@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_head {
  this: np:hasAssertion dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_assertion ;
    np:hasProvenance dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_provenance ;
    np:hasPublicationInfo dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_assertion a np:Assertion .
  dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_provenance a np:Provenance .
  dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_assertion {
  miriam-gene:2067 a ncit:C16612 .
  lld:C0013336 a ncit:C7057 .
  dgn-gda:DGN0c19d01ec80b8be931e347afc059e524 sio:SIO_000628 miriam-gene:2067 , lld:C0013336 ;
    a sio:SIO_001121 .
}
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_provenance {
  dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_assertion dcterms:description "[In addition to the previously reported symptoms of severe runting, abnormalities of liver nuclei and greatly reduced lifespan (which appeared less severe in the truncation mutant), both types of ERCC1-mutant mouse exhibited an absence of subcutaneous fat, early onset of ferritin deposition in the spleen, kidney malfunction, gross abnormalities of ploidy and cytoplasmic invaginations in nuclei of liver and kidney, and compromised NER and cross-link repair.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:9197240 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
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}